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Mismatched Donor Cells to Treat Acute Myeloid Leukemia (ATAC-AML-01)

2017년 8월 28일 업데이트: Elizabeth Krakow, Maisonneuve-Rosemont Hospital

Adoptive Transfer of Alloreactive Cells to Treat Patients With Poor-Prognosis Acute Myeloid Leukemia-01

The purpose of this study is to assess the safety and efficacy of infusing immune cells from a donor as treatment for patients with acute myeloid leukemia that is resistant to chemotherapy or who have experienced relapse. Unlike standard bone marrow or stem cell transplantation which uses donors who are well 'matched' to the patient, this study uses donors whose immune cells are not compatible with the patient. With standard stem cell or bone marrow transplantation, the well-matched immune cells will attack the leukemia but they also attack the patient's organs (a situation called graft-versus-host disease, which can persist in the long term). Our hypothesis is that the mismatched donor cells will fight the leukemia but will then be eliminated from the patient's body, so long-term side effects like graft-versus-host disease should not occur.

연구 개요

상태

알려지지 않은

상세 설명

The ATAC cell therapy product contains unselected, non-mobilized peripheral blood mononuclear cells from related donors who are mismatched to the recipients at 3 or more (out of 6) HLA loci. Cohorts of 3 patients will be treated at each of four pre-specified dose levels (T cells per kg recipient weight). One ATAC infusion is administered 24-48 hours following re-induction chemotherapy (for relapsed or primary refractory AML patients not in remission). In situations where ATAC infusion is not available immediately following re-induction chemotherapy and patients nonetheless achieve complete remission, one ATAC infusion is given 24-48 hours after consolidation chemotherapy.

연구 유형

중재적

등록 (예상)

12

단계

  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Quebec
      • Montreal, Quebec, 캐나다, H1T 3M4
        • 모병
        • Hopital Maisonneuve-Rosemont

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Recipient Inclusion Criteria:

  • Age ≥ 18 years (no upper age limit, but physician discretion is advised)
  • AML that is refractory to 2 courses of induction therapy (that together constitute the 'first-line' therapy) or that has relapsed after a period of morphologic complete remission or morphologic remission with incomplete blood count recovery (CRi)
  • Candidacy for intense induction chemotherapy (ECOG 0-2, adequate renal, liver and cardiac function, absence of uncontrolled infections)
  • Availability of parents, siblings or children who are HLA haploidentical (and not homozygous for the shared haplotype), who are deemed suitable donors after medical evaluation, and who complete peripheral blood mononuclear cell collection
  • No history of autologous or allogeneic stem cell transplant, purine analog chemotherapy or cyclophosphamide, or total body irradiation
  • Ability to comprehend the investigational nature of the study and provide informed consent

Recipient Exclusion Criteria:

  • Acute promyelocytic leukemia (including those with non-classical rearrangements of RARα)
  • History of severe myelodysplastic syndrome clearly preceding the diagnosis of AML (i.e., red cell transfusion dependence or erythropoietin dependence over a 4-month period, or in the absence of a clear cause, any of the following: hemoglobin consistently below 9 g/dL or platelets below 50 x 10^9/L or ANC below 1000/uL on 2 or more occasions 2 weeks apart, or use of G-CSF to maintain the ANC threshold in the absence of infection, in the 3 months preceding the diagnosis of AML). Exception: If ATAC therapy is being considered as a bridge to stem cell transplantation in patients with an available standard transplant donor (familial, unrelated, or cord blood), this exclusion criterion does not apply.
  • Grade 2-3/3 fibrosis in the diagnostic bone marrow biopsy
  • DLCO < 40% predicted
  • Left ventricular ejection fraction < 40% (evaluated by ECHO or MUGA)
  • AST/SGOT > 2.5 x ULN
  • Bilirubin > 1.5 x ULN
  • Creatinine > 1.5 x ULN
  • Creatinine clearance < 50 mL/min
  • HIV positive
  • Major anticipated illness or organ failure incompatible with survival from chemotherapy
  • Concurrent second primary cancer or a prior malignancy that required cytotoxic treatment within the past 12 months, other than cervical carcinoma in-situ or prostate cancer in-situ
  • Severe psychiatric illness or mental deficiency sufficiently severe as to make compliance with the treatment unlikely and informed consent impossible
  • Any congenital or acquired immunodeficiency that would possibly permit permanent engraftment of donor cells
  • Receiving systemic steroid therapy or systemic immunosuppression such as cyclosporine or TNF-inhibitors
  • Prior or concurrent receipt of any marketed or investigational agent deemed on an ad hoc basis to cause immunomodulation, pose a threat of permanent engraftment or increase the risk of GVHD.

Donor inclusion criteria:

  • Mismatched family donor (incompatibility at 3 loci HLA-A, B and DR of the unshared haplotype, or higher-order incompatibility)
  • Age ≥ 16 and ≤ 80 years
  • Fit to undergo apheresis (normal blood counts, normotensive and no history of stroke).
  • Donor has been tested negative for HIV-1, HIV-2, hepatitis B virus (HBV, surface and core antigen), hepatitis C virus, human T-lymphotropic virus types I/II, and Treponema pallidum (syphilis).
  • ECOG performance status of 2 or less.
  • Adequate veins for leukapheresis or agree to placement of a temporary central venous catheter.
  • Donor must provide written informed consent.
  • Where multiple equally-suitable donors are available, sex mismatched donors will be preferred.

Donor exclusion criteria:

  • Medically uncontrolled coronary heart disease
  • Myocardial infarction within the last 3 months
  • History of seizure
  • History of stroke
  • History of malignancy (except basal cell or squamous carcinoma of the skin, or positive PAP smear and subsequent negative follow-up)
  • Presence of a transmissible disease (such as HIV seropositivity)
  • Presence of a major illness or a suspected systemic dysfunction
  • Presence of an an active inflammatory or autoimmune disorder
  • Female donors who are pregnant or nursing

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: ATAC Therapy
Unselected peripheral blood mononuclear cells given 24-48 hours after induction or consolidation chemotherapy
다른 이름들:
  • Unselected Peripheral Blood Mononuclear Cells

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Safety
기간: 60 days (up to 2 years)
Maximum tolerated cell dose: Dose at which < 33% of patients experienced dose-limiting toxicity. If no DLT occurs, then dose titration will stop at a pre-specified number of T cells/kg. Four dose-level cohorts are planned.
60 days (up to 2 years)

2차 결과 측정

결과 측정
기간
Treatment-related mortality
기간: Continuous up to 2 years
Continuous up to 2 years
Non-relapse mortality
기간: Continuous up to 2 years
Continuous up to 2 years
Incidence of graft-versus-host disease
기간: Continuous up to 2 years
Continuous up to 2 years
Duration of cytopenias
기간: Monitored continuously from ATAC infusion until peripheral blood count recovery or maximum 2 years (whichever is earlier)
Monitored continuously from ATAC infusion until peripheral blood count recovery or maximum 2 years (whichever is earlier)
Overall survival
기간: Continuous up to 2 years
Continuous up to 2 years
Complete and incomplete remissions (CR, CRi)
기간: Day 60 post cell infusion
Day 60 post cell infusion
Relapse-free survival
기간: Continuous up to 2 years
Continuous up to 2 years

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 연구 의자: Jean-Sébastien Delisle, MD,PhD, Hôpital Maisonneuve-Rosemont and Université de Montréal
  • 수석 연구원: Elizabeth Krakow, MD, Hôpital Maisonneuve-Rosemont and Université de Montréal

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2012년 9월 1일

기본 완료 (예상)

2018년 12월 1일

연구 완료 (예상)

2018년 12월 1일

연구 등록 날짜

최초 제출

2013년 2월 10일

QC 기준을 충족하는 최초 제출

2013년 2월 13일

처음 게시됨 (추정)

2013년 2월 15일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2017년 8월 30일

QC 기준을 충족하는 마지막 업데이트 제출

2017년 8월 28일

마지막으로 확인됨

2017년 8월 1일

추가 정보

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

급성 골수성 백혈병에 대한 임상 시험

ATAC Therapy에 대한 임상 시험

3
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